Speaker: Dr. Matthew Petersen

Title: Testing, Testing: In Vitro Diagnostics from Biomarkers to Bedside

Format: Hybrid

Objectives:

  1. Describe how FDA classifies and regulates in vitro diagnostics based on intended use and risk. 

  2. Interpret FDA authorization from a clinican's perspective including what clearance/approval does and does not establish. 

  3. Apply these concepts to FDA-authorized sepsis devices. 

Session date: 
09/10/2026 - 12:00pm to 1:00pm EDT
Add to calendar: 
  • 1.00 ABIM MOC 2
  • 1.00 AMA PRA Category 1 Credit™
    The George Washington University School of Medicine and Health Sciences is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
  • 1.00 Completion
Please login or register to take this course.